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ND23191
DNA
from
Whole Blood
Description:
TOURETTE SYNDROME
Affected:
Yes
Gender:
Male
Age:
14
YR
(At Sampling)
Sample Description
Overview
Phenotypic Data
External Links
Overview
Repository
NINDS Repository
Subcollection
Tourette Syndrome
Quantity
3 µg
Quantitation Method
Please see our
FAQ
Biopsy Source
Peripheral vein
Sample Source
DNA from Whole Blood
Race
White
Subject Type
trio
Family Type
NUCLEAR FAMILIES - MORE THAN ONE AFFECTED
Ethnicity
Not Hispanic/Latino
Country of Origin
USA
Family Member
1
Family History
N
Relation to Proband
proband
Species
Homo
sapiens
Common Name
Human
Note
This material represents a finite resource (DNA from Whole Blood)
Phenotypic Data
Demographic Data
Relation to Proband
proband
Age at Sampling
14 YR
Gender
Male
Age of Onset(If not a control)
7 YR
Age at Diagnosis(If not a control)
10 YR
Hispanic or Latino/Not Hispanic or Latino
Not Hispanic/Latino
Racial Category
White
Country
USA
Diagnosed By
No Data
Data Elements
Clinical Element Type: Tourettes
(Baseline)
Primary Lifetime Clinical Diagnosis
Tourette’s Disorder
present
absent
Chronic Multiple Tics
present
absent
Other Tic disorder
present
absent
Unaffected or undiagnosed primary blood relative of proband
yes
no
Symptoms: Motor Tics
present
absent
Symptoms: Vocal/Verbal Tics
present
absent
Age at Tic onset
7 YEARS
Genetic Data of Subject
Mutation/s in subject's DNA (if present, describe)
present
absent
unknown
Secondary Lifetime Clinical Diagnosis
Obsessive compulsive disorder
present
absent
Attention Deficit/Hyperactivity Disorder
present
absent
Other (specify)
present
absent
Optional data
Handedness
Right
Left
Ambidextrous
smoking history
never
former smoker
current smoker
years smoking
No Data
Other family members
Other family members of this person in NINDS repository
yes
no
Notes:
PARENTS - ND23189, ND23190
Family History of TS and related disorders in first degree relatives of subject
Tourette Syndrome or tic disorders
present
absent
Notes:
FATHER ND23189 CMT
Obsessive Compulsive Disorder (OCD)
present
absent
Attention Deficit Hyperactivity Disorder (ADHD)
present
absent
List all first degree relatives and diagnosis (TS, tic disorder, OCD, ADHD)
ND23189 - CMT
Family History of Neurological Disease in first degree relatives
Motor Neuron Disorders, including ALS
present
absent
Parkinson’s disease
present
absent
Epilepsy
present
absent
Notes:
ND23189
Cerebrovascular Disorders, including stroke and aneurysm
present
absent
External Links
NCBI Gene
Gene ID:2973
NCBI GTR
137580 GILLES DE LA TOURETTE SYNDROME; GTS
OMIM
137580 GILLES DE LA TOURETTE SYNDROME; GTS
Omim Description
GILLES DE LA TOURETTE SYNDROME; GTS
TOURETTE SYNDROMECHRONIC MOTOR TICS, INCLUDED
dbGaP Link
phs001380
Culture Protocols
Supplement
-
Pricing
Commercial and Non-U.S.:
$0.00
USD
U.S. Academic or
Non-profit:
$0.00
USD
NINDS Repository Submitter (past or current) and/or Current NINDS Grantee
$0.00
USD
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How to Order
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MTA / Assurance Form
Statement of Research Intent Form
Related Products
Same Family
NINDS2311